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Insertional Mutagenesis in Neurospora Crassa: Cloning and Molecular Analysis of the Preg(+) Gene Controlling the Activity of the Transcriptional Activator Nuc-1

机译:在神经孢子囊中的插入诱变:控制转录激活因子Nuc-1活性的Preg(+)基因的克隆和分子分析。

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摘要

The transcriptional activator NUC-1 controls the transcription of the genes for phosphorus acquisition enzymes, and its activity is regulated by the negative regulatory factors, PREG and PGOV. In this report, we describe the cloning and molecular analysis of the preg(+) gene. In Neurospora crassa, as in higher eukaryotes, transformation frequently results in nonhomologous integration of transforming DNA. Insertion of transforming DNA into host genes mutates the gene and provides a molecular tag for cloning it. We obtained two mutants that have an insertion in the preg(+) and pgov(+) genes, respectively, among 2 X 10(5) transformants. The preg(+) gene was cloned by screening a Neurospora genomic DNA library with DNA sequences flanking the transforming DNA of the rescued plasmid. Northern analysis showed that the transcription of the preg(+) gene is not regulated by phosphate. The carboxy-terminal half of PREG shows strong homology with Saccharomyces cerevisiae PHO80 whose function is analogous to that of PREG. The preg(c) mutations are located in the well conserved residues which may directly interact with the residues in the regulatory domain of NUC-1.
机译:转录激活因子NUC-1控制磷获取酶基因的转录,其活性由负调节因子PREG和PGOV调节。在此报告中,我们描述了preg(+)基因的克隆和分子分析。与高等真核生物一样,在深层孢菌中,转化通常导致转化DNA的非同源整合。将转化DNA插入宿主基因会使该基因发生突变,并为克隆提供了分子标签。我们获得了两个在2 x 10(5)转化子中分别在preg(+)和pgov(+)基因中插入的突变体。通过筛选Neurospora基因组DNA文库,克隆带有被拯救质粒转化DNA的DNA序列,克隆了preg(+)基因。 Northern分析表明,preg(+)基因的转录不受磷酸盐调节。 PREG的羧基末端一半与酿酒酵母PHO80具有很强的同源性,其功能类似于PREG。 preg(c)突变位于保存良好的残基中,可以直接与NUC-1调节域中的残基相互作用。

著录项

  • 期刊名称 Genetics
  • 作者

    S. Kang; R. L. Metzenberg;

  • 作者单位
  • 年(卷),期 1993(133),2
  • 年度 1993
  • 页码 193–202
  • 总页数 10
  • 原文格式 PDF
  • 正文语种
  • 中图分类 遗传学;
  • 关键词

  • 入库时间 2022-08-17 12:09:29

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